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Cigdem Altay

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Turkey

Chemicals & Drugs

Disorders

Living Beings

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DNA Mutational Analysis

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Physiology

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Publications

TOP 3
Onalan Orhan; Balta Gunay; Oto Ali; Kabakci Giray; Tokgozoglu Lale; Aytemir Kudret; Altay Cigdem; Gurgey Aytemiz; Nazli Nasih
Plasminogen activator inhibitor-1 4G4G genotype is associated with myocardial infarction but not with stable coronary artery disease.
Tavil Betul; Sivri Hatice Serapl Kalkanoglu; Coskun Turgay; Gurgey Aytemiz; Ozyurek Emel; Dursun Ali; Tokatli Aysegul; Altay Cigdem; Gumruk Fatma
Haematological findings in children with inborn errors of metabolism.
Gürgey Aytemiz; Aytac Selin; Kanra Guler; Secmeer Gulten; Ceyhan Mehmet; Altay Cigdem
Outcome in children with purpura fulminans: report on 16 patients.

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All Publications

2008: Onalan Orhan; Balta Gunay; Oto Ali; Kabakci Giray; Tokgozoglu Lale; Aytemir Kudret; Altay Cigdem; Gurgey Aytemiz; Nazli Nasih
Plasminogen activator inhibitor-1 4G4G genotype is associated with myocardial infarction but not with stable coronary artery disease.
Journal of thrombosis and thrombolysis 2008;26(3):211-7.
2006: Tavil Betul; Sivri Hatice Serapl Kalkanoglu; Coskun Turgay; Gurgey Aytemiz; Ozyurek Emel; Dursun Ali; Tokatli Aysegul; Altay Cigdem; Gumruk Fatma
Haematological findings in children with inborn errors of metabolism.
Journal of inherited metabolic disease 2006;29(5):607-11.
2005: Gürgey Aytemiz; Aytac Selin; Kanra Guler; Secmeer Gulten; Ceyhan Mehmet; Altay Cigdem
Outcome in children with purpura fulminans: report on 16 patients.
American journal of hematology 2005;80(1):20-5.
2005: Olcay L; Erdemli E; Kesimer M; Büyükasik Y; Okur H; Kalkanoglu H S; Coskun T; Altay C
High cystine in platelets from patients with nephropathic cystinosis: a chemical, ultrastructural, and functional evaluation.
Journal of clinical pathology 2005;58(9):939-45.
2005: Tanner Stephan M; Li Zhongyuan; Perko James D; Oner Cihan; Cetin Mualla; Altay Cigdem; Yurtsever Zekiye; David Karen L; Faivre Laurence; Ismail Essam A; Gräsbeck Ralph; de la Chapelle Albert
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(11):4130-3.
2004: Gurgey Aytemiz; Balta Gunay; Gumruk Fatma; Altay Cigdem
Analysis of some clinical and laboratory aspects of adolescent patients with thrombosis.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(8):657-62.
2004: Sözen M; Karaaslan C; Oner R; Gümrük F; Ozdemir M A; Altay C; Gürgey A; Oner C
Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish family.
American journal of hematology 2004;76(4):378-82.
2004: Unal Selma; Balta Gunay; Duru Feride; Gumruk Fatma; Altay Cigdem; Gurgey Aytemiz
Clinical and laboratory evaluation of Turkish children with thrombosis for homozygous factor V G1691A mutation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(4):343-6.
2003: Balta Gunay; Gumruk Fatma; Akarsu Nurten; Gurgey Aytemiz; Altay Cigdem
Molecular characterization of Turkish patients with pyrimidine 5' nucleotidase-I deficiency.
Blood 2003;102(5):1900-3.
2003: Balta Gunay; Yuksek Nazmiye; Ozyurek Emel; Ertem Ulya; Hicsonmez Gonul; Altay Cigdem; Gurgey Aytemiz
Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia.
American journal of hematology 2003;73(3):154-60.
2003: Birben Esra; Oner Cihan; Oner Reyhan; Altay Cigdem; Gürgey Aytemiz
Identification of an inframe deletion and a missense mutation in the factor XIIIA gene in two Turkish patients.
European journal of haematology 2003;71(1):39-43.
2003: Balta G; Altay C; Gurgey A
Prevalence of PAI-1 gene 4G/5G genotype in Azerbaijan and Kyrgyzstan populations: literature review.
Journal of thrombosis and haemostasis : JTH 2003;1(4):858-9.
2003: Aslan Deniz; Altay Cigdem
Incidence of high erythrocyte count in infants and young children with iron deficiency anemia: re-evaluation of an old parameter.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2003;25(4):303-6.
2002: Aslan Deniz; Gümrük Fatma; Alikasifoglu Mehmet; Altay Cigdem
Serum alpha-fetoprotein level in Fanconi's anemia: evaluation of 33 Turkish patients.
American journal of hematology 2002;71(4):275-8.
2002: Balta Gunay; Altay Cigdem; Gurgey Aytemiz
PAI-1 gene 4G/5G genotype: A risk factor for thrombosis in vessels of internal organs.
American journal of hematology 2002;71(2):89-93.
2002: Birben Esra; Oner Reyhan; Oner Cihan; Gümrük Fatma; Altay Cigdem; Gürgey Aytemiz
Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion.
British journal of haematology 2002;118(1):278-81.
2002: Aslan D; Gümrük F; Gürgey A; Altay C
Importance of RDW value in differential diagnosis of hypochrome anemias.
American journal of hematology 2002;69(1):31-3.
2002: Oner R; Acar C; Oner C; Yenicesu I; Gümrük F; Gürgey A; Altay C
Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patient.
Pediatric hematology and oncology 2002;19(1):39-44.
2001: Birben E; Oner C; Oner R; Mergen H; Yesilipek A; Gümrük F; Gürgey A; Altay C
Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotype.
Hemoglobin 2001;25(4):441-5.
2001: Birben E; Oner R; Oner C; Gümrük F; Gürgey A; Altay C
Homozygosity for Hb E-Saskatoon [beta22(B4)Glu-->Lys] in a Turkish patient.
Hemoglobin 2001;25(4):409-15.
2001: Oner R; Oner C; Birben E; Sözen M; Gümrük F; Gürgey A; Altay C
beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 relative to the beta-globin cap site.
British journal of haematology 2001;115(1):90-4.
2001: Balta G; Gurgey A; Kudayarov D K; Tunc B; Altay C
Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan.
Thrombosis research 2001;101(4):231-4.
2000: Faivre L; Guardiola P; Lewis C; Dokal I; Ebell W; Zatterale A; Altay C; Poole J; Stones D; Kwee M L; van Weel-Sipman M; Havenga C; Morgan N; de Winter J; Digweed M; Savoia A; Pronk J; de Ravel T; Jansen S; Joenje H; Gluckman E; Mathew C G
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.
Blood 2000;96(13):4064-70.
2000: Demuth I; Wlodarski M; Tipping A J; Morgan N V; de Winter J P; Thiel M; Gräsl S; Schindler D; D'Andrea A D; Altay C; Kayserili H; Zatterale A; Kunze J; Ebell W; Mathew C G; Joenje H; Sperling K; Digweed M
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
European journal of human genetics : EJHG 2000;8(11):861-8.
2000: Oner R; Birben E; Acar C; Oner C; Kara A; Gümrük F; Gürgey A; Altay C
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels.
Hemoglobin 2000;24(3):195-201.
2000: Gurgey A; Kudayarov D K; Tuncer M; Parlak H; Altay C
The factor V Leiden and prothrombin G20210A mutations in Kirghiz population.
Thrombosis and haemostasis 2000;84(2):356.
2000: Togrul J; Rustamov R; Gurgey A; Altay S; Altay C
Prevalence of the prothrombin gene G20210A mutation in Azerbaijan.
British journal of haematology 2000;108(4):887-8.
2000: Oner R; Gümrük F; Acar C; Oner C; Gürgey A; Altay C
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.
Haematologica 2000;85(3):320-1.
2000: Gümrük F; Mergen H; Oner R; Ozcebe O; Sayinalp N; Oner C; Gürgey A; Altay C
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family.
Hemoglobin 2000;24(1):23-9.
1999: Gürgey A; Yenicesu I; Kanra T; Ozsoylu S; Altay C; Hiçsönmez G; Yetgin S; Tuncer M; Gümrük F; Cetin M
Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 cases.
The Turkish journal of pediatrics 1999;41(4):467-71.
1999: Koç A; Oner R; Oner C; Aktas D; Sözen M; Tunçbilek E; Altay C
Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient.
Hematology and cell therapy 1999;41(4):187-9.
1999: Oner A F; Gürgey A; Okur H; Kirazli S; Gümrük F; Altay C
Changes of hemostatic factors in patients with hemoglobinopathies.
The Turkish journal of pediatrics 1999;41(3):323-7.
1999: Waisfisz Q; Saar K; Morgan N V; Altay C; Leegwater P A; de Winter J P; Komatsu K; Evans G R; Wegner R D; Reis A; Joenje H; Arwert F; Mathew C G; Pronk J C; Digweed M
The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.
American journal of human genetics 1999;64(5):1400-5.
1999: Altay C; Cetin M
Vitamin B12 absorption test and oral treatment in 14 children with selective vitamin B12 malabsorption.
Pediatric hematology and oncology 1999;16(2):159-63.
1999: Kinik S T; Tuncer A M; Altay C
Transferrin receptor on peripheral blood lymphocytes in iron deficiency anaemia.
British journal of haematology 1999;104(3):494-8.
1999: Wijker M; Morgan N V; Herterich S; van Berkel C G; Tipping A J; Gross H J; Gille J J; Pals G; Savino M; Altay C; Mohan S; Dokal I; Cavenagh J; Marsh J; van Weel M; Ortega J J; Schuler D; Samochatova E; Karwacki M; Bekassy A N; Abecasis M; Ebell W; Kwee M L; de Ravel T; CG Mathew
Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.
European journal of human genetics : EJHG 1999;7(1):52-9.
1999: Koc A; Pronk J C; Alikasifoglu M; Joenje H; Altay C
Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family.
British journal of haematology 1999;104(1):127-30.
1999: Onur O; Sivri A; Gümrük F; Altay C
Beta thalassaemia: a report of 20 children.
Clinical rheumatology 1999;18(1):42-4.
1998: Tezcan I; Tuncer M; Uçkan D; Cetin M; Alikasifoglu M; Ersoy F; Altay C
Allogeneic bone marrow transplantation in Fanconi anemia from Turkey: a report of four cases.
Pediatric transplantation 1998;2(3):236-9.
1998: Altay C; Oner C; Oner R; Gümrük F; Mergen H; Gürgey A
Effect of alpha-gene numbers on the expression of beta-thalassemia intermedia, beta-thalassemia and (delta beta)0-thalassemia traits.
Human heredity 1998;48(3):121-5.
1998: Gümrük F; Gürgey A; Altay C
A case of hypereosinophilic syndrome associated with factor V Leiden mutation and thrombosis.
British journal of haematology 1998;101(1):208-9.
1998: Oner C; Oner R; Birben E; Balkan H; Gümrük F; Gürgey A; Altay C
HB H disease with homozygosity for red cell G6PD deficiency in a Turkish female.
Hemoglobin 1998;22(2):157-60.
1997: Cetin M; Gürgey A; Gümrük F; Altay C
Serum erythropoietin in children with iron deficiency anemia.
The Turkish journal of pediatrics 1997;39(4):459-64.
1997: Lo Ten Foe J R; Kwee M L; Rooimans M A; Oostra A B; Veerman A J; van Weel M; Pauli R M; Shahidi N T; Dokal I; Roberts I; Altay C; Gluckman E; Gibson R A; Mathew C G; Arwert F; Joenje H
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.
European journal of human genetics : EJHG 1997;5(3):137-48.
1997: Altay C; Alikasifoglu M; Kara A; Tunçbilek E; Ozbek N; Schroeder-Kurth T M
Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience.
Clinical genetics 1997;51(5):296-302.
1997: Altay C; Cetin M
Oral treatment in selective vitamin B12 malabsorption.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 1997;19(3):245-6.
1997: Altay C; Oner C; Oner R; Mesci L; Balkan H; Tüzmen S; Basak A N; Gümrük F; Gürgey A
Genotype-phenotype analysis in HbS-beta-thalassemia.
Human heredity 1997;47(3):161-4.
1997: Oner C; Oner R; Balkan H; Gürgey A; Yalçin A; Avcu F; Altay C
Molecular analysis of the Turkish form of deletion-inversion (delta beta)(0) thalassaemia.
British journal of haematology 1997;96(2):229-34.
1997: Oner C; Gürgey A; Oner R; Balkan H; Gümrük F; Baysal E; Altay C
The molecular basis of Hb H disease in Turkey.
Hemoglobin 1997;21(1):41-51.
1996: Smetanina N S; Oner C; Baysal E; Oner R; Bozkurt G; Altay C; Gürgey A; Adekile A D; Gu L H; Huisman T H
The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants.
Biochimica et biophysica acta 1996;1316(3):176-82.
1996: Altay C; Gürgey A; Basak A N; Tadmouri G O; Schroeder-Kurt T
Fanconi aplastic anemia associated with beta-thalassemia trait.
American journal of hematology 1996;52(3):239-40.
1996: Gürgey A; Beksaç S; Gümrük E; Cakar N; Mesçi L; Altay S; Oner C; Altay C
Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experience.
Pediatric hematology and oncology 1996;13(2):163-6.
1996: Oner R; Oner C; Erdem G; Balkan H; Ozdag H; Erkan M; Gümrük F; Gürgey A; Altay C
A novel (delta beta)(0)-thalassemia due to a approximately 30-kb deletion observed in a Turkish family.
Acta haematologica 1996;96(4):232-6.
1995: Gürgey A; Altay C; Gu L H; Leonova J Y; Delibalta A; Oner C; Huisman T H
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrow.
Hemoglobin 1995;19(3-4):165-72.
1995: Cetin M; Kara A; Gürgey A; Gümrük F; Irken G; Yetgin S; Altay C
Congenital hypoplastic anemia in six patients: unusual association of short proximal phalanges with mild anemia.
Pediatric hematology and oncology 1995;12(2):153-8.
1995: Oner C; Oner R; Gürgey A; Altay C
A new Turkish type of beta-thalassaemia major with homozygosity for two non-consecutive 7.6 kb deletions of the psi beta and beta genes and an intact delta gene.
British journal of haematology 1995;89(2):306-12.
1995: Altay C; Cetin M; Gümrük F; Irken G; Yetgin S; Laleli Y
Familial selective vitamin B12 malabsorption (Imerslund-Gräsbeck syndrome) in a pool of Turkish patients.
Pediatric hematology and oncology 1995;12(1):19-28.
1994: Gürgey A; Kalayci O; Gümrük F; Cetin M; Altay C
Convulsion after blood transfusion in four beta-thalassemia intermedia patients.
Pediatric hematology and oncology 1994;11(5):549-52.
1994: Efremov D G; Dimovski A J; Baysal E; Ye Z; Adekile A D; Ribeiro M L; Schiliro G; Altay C; Gürgey A; Efremov G D
Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation.
British journal of haematology 1994;86(4):824-30.
1994: Sayli T R; Basak A N; Gümrük F; Gürgey A; Altay C
Imerslund-Gräsbeck syndrome coexisting with beta-thalassemia trait.
Pediatric hematology and oncology 1994;11(2):223-5.
1994: Duru F; Gürgey A; Cetin M; Kanra T; Altay C
Chronic autoimmune hemolytic anemia in children: a report of four patients.
Journal of medicine 1994;25(3-4):231-40.
1993: Cürük M A; Dimovski A J; Baysal E; Gu L H; Kutlar F; Molchanova T P; Webber B B; Altay C; Gürgey A; Huisman T H
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
American journal of hematology 1993;44(4):270-5.
1993: Mesci L; Gürgey A; Altay C
Recent progress in DNA technology.
The Turkish journal of pediatrics 1993;35(3):239-40.
1993: Gürgey A; Beksaç S; Mesci L; Cakar N; Karakas U; Kutlar A; Altay C
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde I.
The Turkish journal of pediatrics 1993;35(3):159-62.
1993: Gümrük F; Besim A; Altay C
Ghosal haemato-diaphyseal dysplasia: a new disorder.
European journal of pediatrics 1993;152(3):218-21.
1993: Senaati S; Gumruk F U; Delbakhsh P; Balkanci F; Altay C
Gallbladder pathology in pediatric beta-thalassemic patients. A prospective ultrasonographic study.
Pediatric radiology 1993;23(5):357-9.
1992: Duru F; Gürgey A; Oztürk G; Yörükan S; Altay C
Homozygosity for dominant form of hereditary spherocytosis.
British journal of haematology 1992;82(3):596-600.
1992: Gümrük F; Gürgey A; Duru F; Altay C
Reevaluation of iron absorption and serum ferritin in beta-thalassemia intermedia.
Pediatric hematology and oncology 1992;9(4):359-63.
1992: Oner C; Dimovski A J; Olivieri N F; Schiliro G; Codrington J F; Fattoum S; Adekile A D; Oner R; Yüregir G T; Altay C
Beta S haplotypes in various world populations.
Human genetics 1992;89(1):99-104.
1992: Oner C; Dimovski A J; Altay C; Gurgey A; Gu Y C; Huisman T H; Lanclos K D
Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes.
Blood 1992;79(3):813-9.
1992: Gürgey A; Rötig A; Gümrük F; Cemeroglu P; Sarialioglu F; Altay C
Pearson's marrow-pancreas syndrome in 2 Turkish children.
Acta haematologica 1992;87(4):206-9.
1992: Fei Y J; Oner R; Bözkurt G; Gu L H; Altay C; Gurgey A; Fattoum S; Baysal E; Huisman T H
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.
Acta haematologica 1992;88(2-3):82-5.
1991: Kutlar F; Moscoso H; Kiefer C R; Garver F A; Beksaç S; Onderoglu L; Gurgey A; Altay C; Huisman T H
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses.
Journal of chromatography 1991;567(2):359-68.
1991: Altay C; Gurgey A; Oner R; Kutlar A; Kutlar F; Huisman T H
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site.
Hemoglobin 1991;15(4):327-30.
1991: Oner R; Agarwal S; Dimovski A J; Efremov G D; Petkov G H; Altay C; Gurgey A; Huisman T H
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia.
Hemoglobin 1991;15(1-2):67-76.
1990: Oner C; Gurgey A; Altay C; Kutlar F; Huisman T H
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes.
American journal of hematology 1990;34(3):230-1.
1990: Gürgey A; Ozsoylu S; Hiçsönmez G; Irken G; Altay C
Acute lymphoblastic leukemia in a child with hemoglobins S and Q-Iran.
The Turkish journal of pediatrics 1990;32(1):39-41.
1990: Altay C; Gürgey A
Beta-thalassemia intermedia in Turkey.
Annals of the New York Academy of Sciences 1990;612():81-9.
1990: Oner R; Altay C; Gurgey A; Aksoy M; Kilinç Y; Stoming T A; Reese A L; Kutlar A; Kutlar F; Huisman T H
Beta-thalassemia in Turkey.
Hemoglobin 1990;14(1):1-13.
1989: Uysal S; Anlar B; Altay C; Kirazli S
Role of protein C in childhood cerebrovascular occlusive accidents.
European journal of pediatrics 1989;149(3):216-8.
1989: Gonzalez-Redondo J M; Stoming T A; Kutlar A; Kutlar F; Lanclos K D; Howard E F; Fei Y J; Aksoy M; Altay C; Gurgey A
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemia.
Blood 1989;73(6):1705-11.
1989: Kutlar F; Gonzalez-Redondo J M; Kutlar A; Gurgey A; Altay C; Efremov G D; Kleman K; Huisman T H
The levels of zeta, gamma, and delta chains in patients with Hb H disease.
Human genetics 1989;82(2):179-86.
1989: Stoming T A; Stoming G S; Lanclos K D; Fei Y J; Altay C; Kutlar F; Huisman T H
An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene.
Blood 1989;73(1):329-33.
1989: Fei Y J; Kutlar F; Harris H F; Wilson M M; Milana A; Sciacca P; Schiliro G; Masala B; Manca L; Altay C
A search for anomalies in the zeta, alpha, beta, and gamma globin gene arrangements in normal black, Italian, Turkish, and Spanish newborns.
Hemoglobin 1989;13(1):45-65.
1989: Gurgey A; Altay C; Beksaç M S; Bhattacharya R; Kutlar F; Huisman T H
Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family.
Acta haematologica 1989;81(3):169-71.
1989: Kutlar A; Kutlar F; Aksoy M; Gurgey A; Altay C; Wilson J B; Diaz-Chico J C; Hu H; Huisman T H
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemia.
Hemoglobin 1989;13(1):7-16.
1989: Gurgey A; Altay C; Diaz-Chico J C; Kutlar F; Kutlar A; Huisman T H
Molecular heterogeneity of beta-thalassemia intermedia in Turkey.
Acta haematologica 1989;81(1):22-7.
1988: Fei Y J; Stoming T A; Efremov G D; Efremov D G; Battacharia R; Gonzalez-Redondo J M; Altay C; Gurgey A; Huisman T H
Beta-thalassemia due to a T----A mutation within the ATA box.
Biochemical and biophysical research communications 1988;153(2):741-7.
1988: Ceyhan M; Ozalp I; Altay C
High levels of lactate, pyruvate, and alanine in anemic children.
Clinical pediatrics 1988;27(4):206-9.
1988: Diaz-Chico J C; Yang K G; Stoming T A; Efremov D G; Kutlar A; Kutlar F; Aksoy M; Altay C; Gurgey A; Kilinc Y
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes.
Blood 1988;71(1):248-51.
1988: Altay C; Gurgey A; Wilson J B; Hu H; Webber B B; Kutlar F; Huisman T H
Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr.
Hemoglobin 1988;12(1):87-9.
1987: Altay C; Kutlar A; Wilson J B; Webber B B; Huisman T H
Hb P-Nilotic or alpha 2(beta delta)2 in a Turkish family.
Hemoglobin 1987;11(4):395-9.
1986: Aksoy M; Gurgey A; Altay C; Kilinc Y; Carstairs K C; Kutlar A; Chen S S; Webber B B; Wilson J B; Huisman T H
Some notes about Hb Q-India and Hb Q-Iran.
Hemoglobin 1986;10(2):215-9.
1985: Kilinç Y; Kumi M; Gurgey A; Altay C; Webber B B; Wilson J B; Kutlar A; Huisman T H
Hemoglobin O-Padova or alpha(2)30(B11)Glu----Lys beta 2 observed in members of a Turkish family.
Hemoglobin 1985;9(6):621-5.

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